Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Liesbet Deprez"'
Publikováno v:
Contemporary Cardiology ISBN: 9783031245749
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a2f2bef5eb46e86257be71456ab55b0
https://doi.org/10.1007/978-3-031-24575-6_20
https://doi.org/10.1007/978-3-031-24575-6_20
Autor:
Ramona Mögling, Francesca Colavita, Johan Reimerink, Angeliki Melidou, Katrin Leitmeyer, Maria Keramarou, Daniele Lapa, Massimo Francalancia, Jean-Luc Murk, Ann Vossen, Fabrizio Carletti, Boris Hogema, Adam Meijer, Liesbet Deprez, Antonino di Caro, Concetta Castilletti, Chantal BEM Reusken
Publikováno v:
Eurosurveillance, 27(42). EUR CENTRE DIS PREVENTION & CONTROL
Background Countries worldwide are focusing to mitigate the ongoing SARS-CoV-2 pandemic by employing public health measures. Laboratories have a key role in the control of SARS-CoV-2 transmission. Serology for SARS-CoV-2 is of critical importance to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbfa9703769c6ca33d7321d1a673e5a6
https://hdl.handle.net/1887/3514699
https://hdl.handle.net/1887/3514699
Autor:
Samantha Jones, Petr Kocna, Josep Maria Auge, Natasha Djedovic, Liesbet Deprez, Sally C Benton, Erin L. Symonds
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 517
Quantitative faecal immunochemical tests for haemoglobin (FIT) are being used increasingly around the world in colorectal cancer screening programmes, and in patients presenting with lower bowel symptoms to determine who should proceed to further bow
Autor:
Liesbet Deprez, Stefanie Trapmann, Roxana Beaz Hidalgo, Stéphane Mazoua, Philippe Corbisier, Hendrik Emons, Anne-Marie Kortekaas
Publikováno v:
Biomolecular Detection and Quantification
Biomolecular Detection and Quantification, Vol 9, Iss C, Pp 29-39 (2016)
Biomolecular Detection and Quantification, Vol 9, Iss C, Pp 29-39 (2016)
Digital PCR has become the emerging technique for the sequence-specific detection and quantification of nucleic acids for various applications. During the past years, numerous reports on the development of new digital PCR methods have been published.
Autor:
Ferruccio Ceriotti, Tommaso Trenti, Jean Marc Lessinger, F. Javier Gella, Göran Nilsson, Matthias Orth, Liesbet Deprez, Denis Grote-Koska, Rainer Klauke, Ingrid Zegers, Heinz Schimmel, Brigitte Toussaint
Publikováno v:
Clinical chemistry. 64(8)
BACKGROUND Measurement standardization of the catalytic concentration of α-amylase in serum is based on 3 pillars: the primary reference measurement procedure (PRMP), reference laboratories, and suitable certified reference materials (CRMs). Commuta
Autor:
Valérie Taly, Helen C. Parkes, Kenneth D. Cole, Carole A. Foy, Denise M. O'Sullivan, Simon Cowen, Carla Divieto, Hua-Jun He, Sema Akyürek, Sonia Garrigou, Maria Paola Sassi, Muslum Akgoz, Alexandra S. Whale, Tanja Dreo, Nicholas Redshaw, Alison J Woolford, Sang-Ryoul Park, Young-Kyung Bae, Heidi Goenaga-Infante, Raquel Larios, Alison S. Devonshire, Jernej Pavšič, Liesbet Deprez, Jim F. Huggett, Gerwyn M. Jones, Philippe Corbisier, Claire A Bushell
Publikováno v:
Clinical Chemistry
Clinical Chemistry, American Association for Clinical Chemistry, 2018, 64 (9), pp.1296-1307. ⟨10.1373/clinchem.2017.285478⟩
Clinical Chemistry, American Association for Clinical Chemistry, 2018, 64 (9), pp.1296-1307. ⟨10.1373/clinchem.2017.285478⟩
BACKGROUND Genetic testing of tumor tissue and circulating cell-free DNA for somatic variants guides patient treatment of many cancers. Such measurements will be fundamental in the future support of precision medicine. However, there are currently no
Autor:
Samuel F. Berkovic, Philip Holmgren, Dirk Goossens, Jurgen Del-Favero, T Van Dyck, Berten Ceulemans, Kristien Verhaert, Lieven Lagae, Ingrid E. Scheffer, Albena Jordanova, Anna Jansen, Arvid Suls, Liesbet Deprez, P. De Jonghe, Simone C. Yendle, R. Van Coster, Sarah Weckhuysen
Publikováno v:
Neurology
ResearcherID
ResearcherID
Objectives: Heterozygous mutations in STXBP1, encoding the syntaxin binding protein 1, have recently been identified in Ohtahara syndrome, an epileptic encephalopathy with very early onset. In order to explore the phenotypic spectrum associated with
Autor:
Liesbet Deprez, Reana Velizarova, Arvid Suls, Jan Wauters, Albena Jordanova, Ivo Kremensky, P. De Jonghe, Velina Guergueltcheva, L Claes, T Van Dyck, Iglika Yordanova
Publikováno v:
Neurology
Objectives: The aim of this study was to determine the genetic defect in a 4-generational family with an epileptic disorder characterized by febrile and afebrile polymorphic seizures and mild to severe mental retardation by means of analyzing the neu
Autor:
Arvid Suls, Sarah Weckhuysen, André Palmini, Tine Deconinck, Gert Matthijs, Wim Van Paesschen, Katelijne Peeters, L Claes, Peter De Jonghe, Tine Van Dyck, Liesbet Deprez, Kristl G. Claeys
Publikováno v:
Epilepsia
Summary Purpose: Mutations in the ATP1A2 gene have been described in families with familial hemiplegic migraine (FHM). FHM is a variant of migraine with aura characterized by the occurrence of hemiplegia during the aura. Within several FHM families,
Autor:
A Suls, T Van Dyck, Kristl Claeys, W. Van Paesschen, L Claes, Dominique Audenaert, Dirk Goossens, Liesbet Deprez, P. De Jonghe, K. Peeters, Jurgen Del-Favero
Publikováno v:
Neurology
Objective: To map the disease-causing locus in a large Belgian family with occipitotemporal lobe epilepsy associated with migraine with visual aura and to describe the clinical, electrophysiologic, and imaging characteristics. Methods: DNA samples fr